Cefazolin
- Product NDC
- 25021-102
- 11-digit product format
- 250210102
- Labeler code
- 25021
- Product ID
- 25021-102_76e20ece-6f09-4938-9732-3f4776848651
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- cefazolin sodium
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Sagent Pharmaceuticals
- Application
- ANDA065306
- Marketing category
- ANDA
- Marketing start
- 2015-07-01
- Marketing end
- 2024-03-31
- Substance
- CEFAZOLIN SODIUM
- Active strength
- 10 g/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC], Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 25021-102 | CEFAZOLIN (CEFAZOLIN SODIUM) INJECTION, POWDER, FOR SOLUTION [SAGENT PHARMACEUTICALS] | 14 | Legacy NDC | 20200611_48656c70-206d-652c-204f-62692d57616e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 25021-102-69 | 25021010269 | 10 BOTTLE in 1 CARTON (25021-102-69) > 1 INJECTION, POWDER, FOR SOLUTION in 1 BOTTLE | 10 bottle | 2015-07-01 | 0000-00-00 | No | No | Current |
| 25021-102-99 | 25021010299 | 10 BOTTLE in 1 CARTON (25021-102-99) > 1 INJECTION, POWDER, FOR SOLUTION in 1 BOTTLE | 10 bottle | 2009-04-01 | 0000-00-00 | No | No | Current |